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. 2022 Aug 31;55(8):380–388. doi: 10.5483/BMBRep.2022.55.8.092

Table 2.

BTG1 and BTG2 function as a tumor suppressor in various cancers

Type of cancer Observation Mechanism Reference
BL, FL, DLBCL, HBL* BTG1 or BTG2 are frequently mutated or deleted (57, 58, 61, 68-71)
ALL Deletion of BTG1 can be a cancer driver gene in leukemogenesis Excessive proliferation due to deletion of BTG1 where RAG1/RAG2 mediated recombination occurs (62)
AML BTG1 is downregulated Ectopic expression of BTG1inhibits proliferation (72)
Liver cancer BTG2 expression is downregulated BTG1 is downregulated by miR-511 overexpression, promoting proliferation of hepatoma cells (52)
BTG1 expression is downregulated (73)
Breast cancer BTG1 expression is downregulated (40)
BTG2 can affect radiation-induced apoptosis Lack of BTG2 induces overexpression of cyclin D1 (9)
Ovarian cancer Downregulation of BTG2 is associated with poor prognosis BTG2 inhibits proliferation and cell-cycle via AKT and ERK signaling (74)
Laryngeal carcinoma BTG2 expression is downregulated BTG2 is suppressed via miR-21 (75)
Gastric cancer BTG2 expression is downregulated BTG2 is suppressed via miR-27a-3p (76)
Colorectal cancer BTG1 expression is downregulated Post-transcriptional suppression of BTG1 by miR-22 might balance between autophagy and apoptosis (51)
Lung epithelial cancer Ectopic expression of BTG2 inhibits the growth, proliferation By reducing the expression of cyclin D1, MMP-1 and MMP-2 (27)
Bladder cancer Ectopic expression of BTG2 induces a switch from senescence to apoptosis By translocating of p53 protein (48)

*BL: Burkitt lymphoma, FL: Follicular lymphoma, HBL: High-grade B cell lymphoma, DLBCL: diffuse large B-cell lymphoma, ALL: Acute lymphocytic leukemia, AML: Acute myeloid leukemia.